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BioWorld - Monday, April 13, 2026
Home » Topics » Regulatory » EMA

EMA
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FDA clears design of phase III oritavancin trials SOLO-1 and -2

Dec. 1, 2010

New Juvista formulation for children significantly improves scar appearance

Nov. 23, 2010

CIS Bio withdraws E.U. marketing authorization for NeoSpect

Nov. 23, 2010

EMA's COMP recommends orphan status for paquinimod in systemic sclerosis

Nov. 18, 2010

EMA accepts Pixuvri MAA for non-Hodgkin's lymphoma for review

Nov. 18, 2010

Roche reports on third quarter of 2010

Nov. 18, 2010

EMA approves Cell Therapeutics' pediatric investigation plan for Pixuvri

Nov. 17, 2010

EMA orphan drug status for SBC-102 in LAL deficiency / News in Context

Nov. 17, 2010

EMA committee recommends orphan drug status for ThermoDox in primary liver cancer

Nov. 12, 2010

Schering-Plough Europe withdraws MAA for Zenhale

Nov. 11, 2010
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